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Related to Thalassemia: Thalassemia minor


A hereditary form of hemolytic anemia resulting from a defective synthesis of hemoglobin: thalassemia major is the homozygous state accompanied by clinical illness, and thalassemia minor is the heterozygous state and may not have evident clinical manifestations. Also known as Mediterranean anemia.



(also thalassanemia), a familial hemolytic anemia, first detected in 1925 among inhabitants of the Mediterranean region. Thalassemia is caused by disturbances in hemoglobin synthesis.

References in periodicals archive ?
The blood is destined for people suffering from thalassemia, haemaphilia, and other blood disorders.
in 2007, thalassemia-specific consultation showed to be highly effective in reducing the birth rate of children afflicted with [beta] thalassemia major (14).
They stressed the need that through legislation Thalassemia screening test be made compulsory for couples before getting married so that the fatal disease could be overcome.
Patients suffering from thalassemia should be constantly monitored by a specialist in order to manage their condition long-term.
The Sultan Bin Khalifa International Thalassemia Award is a unique initiative and a commitment of Dr Shaikh Sultan bin Khalifa Al Nahyan, Advisor to the UAE President, and his family to improve the quality of life patients with thalassemia and other inherited blood disorders .
He had over 300 publications, mainly on different types of thalassemia and their molecular genetics.
The two branches offer free of charge medical services to thalassemia patients, of which there are around 1,500.
A review of the Thalassemia products under development by companies and universities/research institutes based on information derived from company and industry-specific sources.
Thalassemia major (TM) is an inherited blood disorder which is characterized by reduced synthesis of one or more of the globins that form the hemoglobin tetramer.
Thalassemia was first described in a child with deep anemia, splenomegamia and characteristic bone changes in 1925 by Thomas Cooley and Peael Lee (9).
The carrier status of certain hemoglobinopathies and thalassemias is especially critical in the prenatal period where the hemoglobin phenotype of the partner may be of importance if a homozygous hemoglobinopathy or severe thalassemia in the resulting fetus is a possibility.
Christofias, visited on Thursday the Thalassemia International Federation (TIF) headquarters and Thalassemia Center at Makarios Hospital in Nicosia, where she inspected Cyprus pioneering experience in combating this disease.